ClinVar Miner

List of variants in gene ATR reported as uncertain significance

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Total variants: 95
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HGVS dbSNP
NM_001184.3(ATR):c.-91C>G rs189343119
NM_001184.4(ATR):c.*72T>G rs750327573
NM_001184.4(ATR):c.-29_-9delinsT rs886058060
NM_001184.4(ATR):c.1006C>T (p.Arg336Trp) rs886058056
NM_001184.4(ATR):c.1318C>T (p.Pro440Ser) rs535140939
NM_001184.4(ATR):c.1350-3T>C rs587783323
NM_001184.4(ATR):c.1358_1359del (p.His453fs) rs886044646
NM_001184.4(ATR):c.152-9T>C rs748613519
NM_001184.4(ATR):c.1626A>G (p.Lys542=) rs762125386
NM_001184.4(ATR):c.1784C>T (p.Ser595Leu) rs747451103
NM_001184.4(ATR):c.1885+7G>A rs74282951
NM_001184.4(ATR):c.1903C>T (p.Arg635Ter) rs1378333855
NM_001184.4(ATR):c.190A>G (p.Thr64Ala) rs35306038
NM_001184.4(ATR):c.196G>A (p.Val66Met) rs758564083
NM_001184.4(ATR):c.2092G>A (p.Asp698Asn) rs1553770633
NM_001184.4(ATR):c.2205C>T (p.His735=) rs148955716
NM_001184.4(ATR):c.2226T>C (p.Cys742=) rs147895945
NM_001184.4(ATR):c.2242A>G (p.Thr748Ala) rs879255363
NM_001184.4(ATR):c.225C>T (p.Ile75=) rs886058059
NM_001184.4(ATR):c.2290A>G (p.Lys764Glu) rs77208665
NM_001184.4(ATR):c.2503T>C (p.Leu835=) rs377134163
NM_001184.4(ATR):c.2532+4G>A rs190596919
NM_001184.4(ATR):c.260G>T (p.Ser87Ile) rs200407265
NM_001184.4(ATR):c.2634-1G>A rs372271245
NM_001184.4(ATR):c.2653G>A (p.Val885Ile) rs141606250
NM_001184.4(ATR):c.2688G>A (p.Leu896=) rs117926957
NM_001184.4(ATR):c.2776T>C (p.Phe926Leu) rs141783863
NM_001184.4(ATR):c.289A>T (p.Ile97Phe) rs138473993
NM_001184.4(ATR):c.292+15T>G rs886058058
NM_001184.4(ATR):c.305G>T (p.Trp102Leu) rs794727632
NM_001184.4(ATR):c.3152G>A (p.Arg1051His)
NM_001184.4(ATR):c.3241C>T (p.Leu1081=) rs139173669
NM_001184.4(ATR):c.325C>T (p.Arg109Trp) rs146405935
NM_001184.4(ATR):c.3424A>G (p.Ser1142Gly) rs149008479
NM_001184.4(ATR):c.3497A>C (p.His1166Pro) rs201438783
NM_001184.4(ATR):c.3614A>G (p.His1205Arg) rs1553767201
NM_001184.4(ATR):c.3642T>C (p.His1214=) rs139078985
NM_001184.4(ATR):c.3799G>A (p.Val1267Ile) rs377689383
NM_001184.4(ATR):c.3945+2dup rs537031994
NM_001184.4(ATR):c.3952del (p.Lys1317_Leu1318insTer) rs869312789
NM_001184.4(ATR):c.4153-21dup rs112116713
NM_001184.4(ATR):c.4218G>A (p.Ala1406=) rs770181975
NM_001184.4(ATR):c.423T>C (p.Ile141=) rs10935466
NM_001184.4(ATR):c.4306A>G (p.Asn1436Asp) rs587783328
NM_001184.4(ATR):c.431T>G (p.Val144Gly) rs749942139
NM_001184.4(ATR):c.4323A>G (p.Gln1441=) rs56100509
NM_001184.4(ATR):c.4351C>T (p.Arg1451Trp) rs148064542
NM_001184.4(ATR):c.436A>G (p.Thr146Ala) rs765018743
NM_001184.4(ATR):c.4376A>G (p.Asn1459Ser) rs144591613
NM_001184.4(ATR):c.437C>A (p.Thr146Lys) rs368592452
NM_001184.4(ATR):c.4382+6T>C rs758074436
NM_001184.4(ATR):c.4405A>G (p.Thr1469Ala) rs78895258
NM_001184.4(ATR):c.4407C>T (p.Thr1469=) rs201300027
NM_001184.4(ATR):c.4509A>T (p.Arg1503=) rs398123602
NM_001184.4(ATR):c.4576A>G (p.Ile1526Val) rs34124242
NM_001184.4(ATR):c.4641+15C>T rs200619976
NM_001184.4(ATR):c.4677C>T (p.Asp1559=) rs112726878
NM_001184.4(ATR):c.4764C>T (p.Leu1588=) rs142240637
NM_001184.4(ATR):c.4820G>A (p.Ser1607Asn) rs55724025
NM_001184.4(ATR):c.4846T>G (p.Ser1616Ala) rs201492267
NM_001184.4(ATR):c.489T>C (p.Asn163=) rs886058057
NM_001184.4(ATR):c.4957C>T (p.Arg1653Ter) rs778813551
NM_001184.4(ATR):c.5052T>C (p.His1684=) rs150810277
NM_001184.4(ATR):c.5257A>G (p.Ile1753Val) rs143806447
NM_001184.4(ATR):c.5305G>C (p.Glu1769Gln) rs376811787
NM_001184.4(ATR):c.5349G>T (p.Gln1783His) rs886058055
NM_001184.4(ATR):c.5572T>C (p.Cys1858Arg) rs367898142
NM_001184.4(ATR):c.5732A>G (p.Asn1911Ser) rs587783334
NM_001184.4(ATR):c.5739-11_5739-4del rs797045404
NM_001184.4(ATR):c.5739-14G>T rs587783335
NM_001184.4(ATR):c.5739-14_5739-6delinsT rs886058054
NM_001184.4(ATR):c.5739-14_5739-7del rs878853001
NM_001184.4(ATR):c.5899-8del rs538488507
NM_001184.4(ATR):c.59+4G>A rs758046042
NM_001184.4(ATR):c.5900G>A (p.Gly1967Asp) rs751198306
NM_001184.4(ATR):c.5987T>C (p.Met1996Thr) rs150339560
NM_001184.4(ATR):c.6078+10T>C rs762754313
NM_001184.4(ATR):c.6079-14G>A rs886058053
NM_001184.4(ATR):c.6090G>A (p.Ala2030=) rs201988169
NM_001184.4(ATR):c.6197G>A (p.Arg2066Gln) rs886058052
NM_001184.4(ATR):c.6221+3G>A rs200980335
NM_001184.4(ATR):c.6226C>G (p.Leu2076Val) rs372864251
NM_001184.4(ATR):c.6259A>G (p.Met2087Val) rs757353909
NM_001184.4(ATR):c.6394T>G (p.Tyr2132Asp) rs28910273
NM_001184.4(ATR):c.6896T>C (p.Met2299Thr) rs145119827
NM_001184.4(ATR):c.6960G>A (p.Lys2320=) rs752654793
NM_001184.4(ATR):c.6961T>C (p.Phe2321Leu) rs587783338
NM_001184.4(ATR):c.7041+4G>C rs113544835
NM_001184.4(ATR):c.7041+8G>A rs201106004
NM_001184.4(ATR):c.7220G>A (p.Arg2407His) rs778835776
NM_001184.4(ATR):c.7356_7358TAG[3] (p.Ser2453dup) rs756975919
NM_001184.4(ATR):c.7471G>A (p.Val2491Ile) rs556313656
NM_001184.4(ATR):c.7667C>G (p.Thr2556Ser) rs200490116
NM_001184.4(ATR):c.7725G>A (p.Ala2575=) rs587783340
NM_001184.4(ATR):c.992A>G (p.Asp331Gly) rs150008448

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